Executive / Sr. Executive – QC / QA

Job Description

Title: Executive / Sr. Executive – QC / QA

Company Name: Salton Pharmaceuticals Ltd.

Vacancy: --

Age: At most 30 years

Job Location: Anywhere in Bangladesh

Salary: --

Experience:

• 2 to 5 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies

• Bachelor of Pharmacy (B.Pharm)
• Master of Pharmacy (M.Pharm)

• Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm) from a recognized university.

• Candidates must have a valid registration with the Pharmacy Council of Bangladesh, where applicable.

• 2 to 5 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies

• Age At most 30 years

• Preferably within 30 years, depending on qualifications and relevant experience.

• 2–5 years of relevant experience in Quality Control and/or Quality Assurance in a pharmaceutical manufacturing company.

• Experience in GMP-compliant pharmaceutical manufacturing will be highly preferred.

• Candidates with hands-on experience in QC laboratory activities, documentation, validation, deviation, CAPA, change control, SOP, and batch-related activities will receive preference.

• Good knowledge of WHO-GMP and pharmaceutical Quality Management Systems.

• Strong understanding of pharmaceutical manufacturing and quality documentation.

• Good analytical, problem-solving, and decision-making skills.

• Strong communication and interpersonal skills.

• Ability to work independently as well as in a team.

• Good computer literacy, particularly Microsoft Office applications.

• Ability to work under pressure and meet deadlines.

Context:

Salton Pharmaceuticals Limited, a growing pharmaceutical manufacturing company, is looking for competent, motivated, and career-oriented professionals to join its Quality Control (QC) / Quality Assurance (QA) Department at our Factory Site.

Job Location: Factory Site

Number of Vacancies: As per organizational requirement

Key Responsibilities

For Quality Control (QC):

• Perform testing and analysis of raw materials, packaging materials, in-process materials, finished products, and stability samples.

• Ensure laboratory activities are performed in accordance with approved specifications, STPs, SOPs, and GMP requirements.

• Review analytical results, laboratory records, worksheets, and related documentation.

• Handle laboratory investigations, OOS/OOT results, and support root-cause analysis.

• Maintain proper documentation and ensure data integrity in QC activities.

• Ensure proper calibration, maintenance, and qualification of laboratory instruments.

• Coordinate with Production, QA, R&D, and other relevant departments when required.

For Quality Assurance (QA):

• Ensure compliance with GMP, GLP, GDP, and applicable regulatory requirements.

• Review batch manufacturing and packaging records and support batch release activities.

• Manage and review deviations, CAPA, change controls, OOS/OOT investigations, and related quality documentation.

• Prepare, review, and control SOPs and other quality documents.

• Support validation and qualification activities, including process validation, cleaning validation, equipment qualification, and related activities.

• Participate in internal audits, self-inspections, vendor qualification, and regulatory inspections.

• Monitor compliance with approved procedures and quality management system requirements.

• Coordinate with Production, QC, R&D, Engineering, and other departments to ensure effective implementation of the Quality Management System.

• Attractive salary package commensurate with qualifications and experience.

• Festival bonuses and other benefits as per company policy.

• Opportunity for professional growth and career development.

• A professional and quality-driven working environment.